Armstrong Sara A, Sese Denise, Menon Aravind
Internal Medicine, Medical University of South Carolina, Charleston, USA.
Pulmonary and Critical Care Medicine, Medical University of South Carolina, Charleston, USA.
Cureus. 2025 Apr 1;17(4):e81584. doi: 10.7759/cureus.81584. eCollection 2025 Apr.
Melanoma differentiation-associated gene 5 (MDA-5) autoimmunity has been increasingly recognized in association with interstitial lung disease (ILD), particularly in the context of viral infections. While MDA-5 ILD is typically rapidly progressive with high mortality, emerging evidence suggests that COVID-19 may induce a distinct, more indolent phenotype. We report two cases of MDA-5 ILD following COVID-19 infection with a slowly progressive course. In Case 1, an 87-year-old woman with a history of breast cancer, chronic obstructive pulmonary disease (COPD), and a prior COVID-19 infection developed progressive dyspnea. Imaging revealed new-onset ILD with subpleural reticulations and traction bronchiectasis. A myositis antibody panel was positive for MDA-5 autoantibodies. She was diagnosed with MDA-5 ILD and initiated on corticosteroids, later transitioned to mycophenolate. She has since remained clinically stable over the past two years. In Case 2, an 84-year-old man with a history of smoking and asbestos exposure developed severe dyspnea and hypoxia after a mild COVID-19 infection. CT imaging revealed diffuse ground-glass opacities and interlobular septal thickening. He was diagnosed with MDA-5 ILD and Group 1 and 3 pulmonary hypertension. He was treated with mycophenolate and pulmonary vasodilators, leading to symptom stabilization. These cases illustrate a possible post-COVID-19 endotype of MDA-5 ILD that follows a slower disease trajectory, distinct from the classical rapidly progressive phenotype. The association between viral infections and MDA-5 autoimmunity is supported by prior studies demonstrating viral-induced interferon signaling and MDA-5 gene activation. Given the indolent nature of disease progression in our patients, a tailored immunosuppressive approach was pursued, resulting in the stabilization of symptoms and pulmonary function. These cases contribute to the growing recognition of post-COVID-19 MDA-5 ILD as a unique clinical entity. Further research is needed to elucidate the precise mechanisms underlying virus-induced autoimmunity and to guide treatment strategies for this emerging ILD subtype.
黑色素瘤分化相关基因5(MDA-5)自身免疫与间质性肺疾病(ILD)的关联日益受到关注,尤其是在病毒感染的背景下。虽然MDA-5相关性ILD通常进展迅速且死亡率高,但新出现的证据表明,新型冠状病毒肺炎(COVID-19)可能引发一种不同的、更为隐匿的表型。我们报告了2例COVID-19感染后发生的MDA-5相关性ILD病例,其病程进展缓慢。病例1为一名87岁女性,有乳腺癌、慢性阻塞性肺疾病(COPD)病史,曾感染过COVID-19,出现进行性呼吸困难。影像学检查显示新发ILD,伴有胸膜下网状影和牵拉性支气管扩张。肌炎抗体检测显示MDA-5自身抗体呈阳性。她被诊断为MDA-5相关性ILD,并开始使用糖皮质激素治疗,随后改用霉酚酸酯。在过去两年里,她的病情一直保持临床稳定。病例2为一名84岁男性,有吸烟和石棉接触史,在轻度COVID-19感染后出现严重呼吸困难和低氧血症。CT检查显示弥漫性磨玻璃影和小叶间隔增厚。他被诊断为MDA-5相关性ILD以及1型和3型肺动脉高压。他接受了霉酚酸酯和肺血管扩张剂治疗,症状得以稳定。这些病例说明了COVID-19感染后MDA-5相关性ILD可能存在一种病程较慢的亚型,与典型的快速进展型表型不同。先前的研究表明病毒可诱导干扰素信号传导和MDA-5基因激活,支持了病毒感染与MDA-5自身免疫之间的关联。鉴于我们患者疾病进展较为隐匿,我们采取了针对性的免疫抑制方法,从而使症状和肺功能得以稳定。这些病例有助于人们越来越认识到COVID-19感染后MDA-5相关性ILD是一种独特的临床实体。需要进一步研究以阐明病毒诱导自身免疫的确切机制,并指导针对这种新出现的ILD亚型的治疗策略。